August 8th, 2018: Understanding and Remembrance Day for Severe ME
Have you heard of our Severe Myalgic Encephalomyelitis Day of Understanding and Remembrance? Please join Jody Smith in observing this day and honoring the 25% of those with ME/CFS who are most severely ill.
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Discussion in 'General Symptoms' started by Fuzzyhead, Oct 11, 2018.

  1. Fuzzyhead

    Fuzzyhead Senior Member

    Been ill 18years and had all sorts of symptoms over the years. Ive had an ms scare because of a few brain lesions. Tested weak positive for lyme and suffered health anxiety along the way. My symptoms are back full force, i have a left sided headache, left temple twitching, my left eye feels odd and strained, off balance, my right arm and leg feel different, cant think straight, have to think before i speak because i feel i will muddle my words, awful brain fog, crying and anxious. Convinced myself its a brain tumour AGAIN because it feels different this time. Only ever been given m.e diagnosis.
  2. Hufsamor

    Hufsamor Senior Member

    Big hug:hug:
    Anxiety is no fun at all.
    And all your pain?
    My heart goes to you
    I hope you soon will have a better day and get some relief :heart:

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